HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Methylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Phthalic Acid | HCID 1017 | 40% |
| Product | Phthalic Anhydride | HCID 6811 | 10% |
| Product | 2-Methylbenzoic acid | HCID 8373 | 46% |
Reaction Steps
To 25 milliliters of acetic acid were added 1.06 grams (10 millimoles) of o-xylene, 0.16 gram (1 millimole) of N-hydroxyphthalimide and 0.018 gram (0.05 millimole) of acetylacetonatocobalt(II) Co(AA)2, and the resultant mixture was stirred in an oxygen atmosphere at a temperature of 100° C. for 6 hours. With a transformation rate of 98%, o-xylene was transformed into phthalic acid (yield 40%), o-methylbenzoic acid (yield 46%) and phthalic anhydride (yield 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958821 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-76af2f4e2daa45b8b8837d62a513061f |
| Source note | uspto-grants-1999_09 |